Difference between revisions of "Team:NCTU Formosa/Design"

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   <h2>Probe: scFv from targeted drug</h2>
 
   <h2>Probe: scFv from targeted drug</h2>
 
<p>
 
<p>
In order to provide doctors with new, direct, and innovative methods in determining the usage of monoclonal-antibody-targeted drugs ,we redesigned the FDA approved monoclonal antibody targeted drugs, such as Bevacizumab (Avastin® anti-VEGF)<sup>[1]</sup>, Cetuximab (Erbitux® anti-EGFR) <sup>[2]</sup> and Trastuzumab (Herceptin® anti-HER2)<sup>[3]</sup> into scFv as probes.
+
In order to provide doctors with new, direct, and innovative methods in determining the usage of monoclonal-antibody-targeted drugs, we redesigned the FDA approved monoclonal antibody targeted drugs, such as Bevacizumab (Avastin® anti-VEGF) <sup>[1]</sup>, Cetuximab (Erbitux® anti-EGFR) <sup>[2]</sup> and Trastuzumab (Herceptin® anti-HER2) <sup>[3]</sup> into scFv as probes.
 
</p>
 
</p>
 
<div class="image">
 
<div class="image">
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</div>
 
</div>
  
<p>Each distinct scFv of targeted drug is displayed on the surfaces of <i>E. coli</i>. ScFv from targeted drugs can specifically detect target molecules. </p>
+
<p>Each distinct scFv of targeted drug is displayed on the surfaces of <i>E.coli</i>. ScFv from targeted drugs can specifically detect target molecules. </p>
 
<p>Furthermore, as APOllO E.Cotector expressed scFv and color signal at the same time, the specific molecules that correspond to those scFv can be identified by different colors, hence offering an accurate prescription of monoclonal antibody targeted drug.</p>
 
<p>Furthermore, as APOllO E.Cotector expressed scFv and color signal at the same time, the specific molecules that correspond to those scFv can be identified by different colors, hence offering an accurate prescription of monoclonal antibody targeted drug.</p>
  
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<h2>Transmembrane Protein of scFv</h2>
 
<h2>Transmembrane Protein of scFv</h2>
   <p>To display scFv on the surface of <i>E.coli</i>, we use a transmembrane protein. The transmembrane protein is composed of lipoprotein (Lpp) and outer membrane protein A (OmpA).</p>
+
   <p>To display scFv on the surface of <i>E.coli</i>, we use a transmembrane protein. The transmembrane protein is composed of lipoprotein (Lpp) and outer membrane protein A (OmpA) .</p>
  
 
<div class="image">
 
<div class="image">
 
   <img src="https://static.igem.org/mediawiki/2015/3/30/Figure_3_Transmembrane_Protein_Lpp_OmpA.png" height="200px"><br><br>
 
   <img src="https://static.igem.org/mediawiki/2015/3/30/Figure_3_Transmembrane_Protein_Lpp_OmpA.png" height="200px"><br><br>
   Figure 5. Figure 6. Transmembrane protein: Lpp-OmpA is composed of lipoprotein (Lpp)and outer membrane protein A (OmpA).
+
   Figure 5. Figure 6. Transmembrane protein: Lpp-OmpA is composed of lipoprotein (Lpp) and outer membrane protein A (OmpA) .
 
   </div>
 
   </div>
 
    
 
    
 
    
 
    
   <p>Lpp-OmpA was designed as a fusion protein consisting of the signal sequence and first 9 amino acids of Lpp, residue 46~159 of OmpA. The Lpp of the N-terminal of this fusion protein targets the protein on the membrane while the transmembrane domain of OmpA serves as an anchor. ScFv is on the externally exposed loops of C-terminal of OmpA, which can be anchored to the outer membrane. Between the OmpA and scFv, there is a cut site of restriction enzyme called NcoI. With this cut site, the linked scFv can be easily changed like a cassette.<sup>[1]</sup></p>
+
   <p>Lpp-OmpA was designed as a fusion protein consisting of the signal sequence and first 9 amino acids of Lpp, residue 46~159 of OmpA. The Lpp of the N-terminal of this fusion protein targets the protein on the membrane while the transmembrane domain of OmpA serves as an anchor. ScFv is on the externally exposed loops of C-terminal of OmpA, which can be anchored to the outer membrane. Between the OmpA and scFv, there is a cutting site of restriction enzyme called <i>Nco</i>I. With this cutting site, the linked scFv can be easily changed like a cassette. <sup>[1]</sup></p>
  
 
  <div class="image">
 
  <div class="image">
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<img src="https://static.igem.org/mediawiki/2015/b/b4/Lpp-OmpA_NcoI.png" height="70px">
 
<img src="https://static.igem.org/mediawiki/2015/b/b4/Lpp-OmpA_NcoI.png" height="70px">
 
<img src="https://static.igem.org/mediawiki/2015/a/ab/Ncol_scFv.png" height="85px"> <br><br>
 
<img src="https://static.igem.org/mediawiki/2015/a/ab/Ncol_scFv.png" height="85px"> <br><br>
   Figure 7. To change the scFv sequence easily, we designed the NcoI restriction site between Lpp-Omp A and scFv. When designing XbaI-SpeI restriction site between Lpp-OmpA and scFv, it cause mixed site. Therefore, NcoI restriction site rather than EX-SP restriction site was designed.
+
   Figure 7. To change the scFv sequence easily, we designed the <i>NcoI</i> restriction site between Lpp-Omp A and scFv. When designing XbaI-SpeI restriction site between Lpp-OmpA and scFv, it cause mixed site. Therefore, <i>Nco</i>I restriction site rather than EX-SP restriction site was designed.
  
  
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   <h2>Color Signal</h2>
 
   <h2>Color Signal</h2>
<p>The color signals that we have selected are florescence proteins and chromoproteins. Cooperating with iGEM, all of resources were from the giant registry of iGEM which is accessible to every iGEMer.     
+
<p>The color signals that we have selected are fluorescence proteins and chromoproteins. Cooperating with iGEM, all of resources were from the giant registry of iGEM which is accessible to every iGEMer.     
APOllO utilized the red florescent protein <a href="http://parts.igem.org/Part:BBa_E1010">BBa_E1010</a>, the green fluorescent protein <a href="http://parts.igem.org/Part:BBa_E0040">BBa_E0040</a>, the blue fluorescent protein <a href="http://parts.igem.org/Part:BBa_K592100">BBa_K592100</a> , and the blue chromoprotein <a href="http://parts.igem.org/Part:BBa_K592009">BBa_K592009</a>.</p>
+
APOllO utilized the red flourescent protein <a href="http://parts.igem.org/Part:BBa_E1010">BBa_E1010</a>, the green fluorescent protein <a href="http://parts.igem.org/Part:BBa_E0040">BBa_E0040</a>, the blue fluorescent protein <a href="http://parts.igem.org/Part:BBa_K592100">BBa_K592100</a> , and the blue chromoprotein <a href="http://parts.igem.org/Part:BBa_K592009">BBa_K592009</a>.</p>
  
 
<p><a href="https://2015.igem.org/Team:NCTU_Formosa/Results">Jump to Results</a></p>
 
<p><a href="https://2015.igem.org/Team:NCTU_Formosa/Results">Jump to Results</a></p>
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<p>Another plasmid is gold binding polypeptide, abbreviated as GBP. APOllO may display GBP on the surface of <i>E. coli</i> for binding on gold surface.</p>
 
<p>Another plasmid is gold binding polypeptide, abbreviated as GBP. APOllO may display GBP on the surface of <i>E. coli</i> for binding on gold surface.</p>
 
    
 
    
  <p>GBP was designed with the three-repeated following 14 amino acid sequences: [MHGKTQATSGTIQS]. The binding sequence of GBP does not contain cysteine which can form a covalent thiol linkage with gold, the linkage to the gold surface in Self-Assembled Monolayers (SAMs)<sup>[2]</sup>.</P>
+
  <p>GBP was designed with the three-repeated following 14 amino acid sequences: [MHGKTQATSGTIQS]. The binding sequence of GBP does not contain cysteine which can form a covalent thiol linkage with gold, the linkage to the gold surface in Self-Assembled Monolayers (SAMs) <sup>[2]</sup>.</P>
 
<p>The mechanism of the connection between GBP and gold metal plane remains unknown. By using Molecular Dynamics (MD), it indicates that GBP, with an antiparallel β-sheet structure, can recognize gold surface via OH-binding. It is likely that the hydroxyl, together with amine, ligands on GBP recognize the atomic lattice of gold, aligning the molecule along the variants of a six-fold axis on the Au (111) surface <sup>[3]</sup>.</p>
 
<p>The mechanism of the connection between GBP and gold metal plane remains unknown. By using Molecular Dynamics (MD), it indicates that GBP, with an antiparallel β-sheet structure, can recognize gold surface via OH-binding. It is likely that the hydroxyl, together with amine, ligands on GBP recognize the atomic lattice of gold, aligning the molecule along the variants of a six-fold axis on the Au (111) surface <sup>[3]</sup>.</p>
  

Revision as of 15:31, 18 September 2015

Design

Core of APOllO E.Cotector: Customization

By utilizing the concept of cotransformation, APOllO can offer various E. Cotectors with scFv, color signal or GBP and even any desired combination. Therefore, APOllO could customize the E.Cotector to satisfy the need of various detection platforms.



Figure 1. With the co-transform technique, we can insert any scFv or signal-related genetic sequences we want into the E.coli, and create a customized platform ─ the APOllO E.Cotector.

Single Chain Variable Fragment

Probe: scFv from targeted drug

In order to provide doctors with new, direct, and innovative methods in determining the usage of monoclonal-antibody-targeted drugs, we redesigned the FDA approved monoclonal antibody targeted drugs, such as Bevacizumab (Avastin® anti-VEGF) [1], Cetuximab (Erbitux® anti-EGFR) [2] and Trastuzumab (Herceptin® anti-HER2) [3] into scFv as probes.



Figure 3. We design the platform to detect multimarkers as the reference for applying the combination therapy.

Each distinct scFv of targeted drug is displayed on the surfaces of E.coli. ScFv from targeted drugs can specifically detect target molecules.

Furthermore, as APOllO E.Cotector expressed scFv and color signal at the same time, the specific molecules that correspond to those scFv can be identified by different colors, hence offering an accurate prescription of monoclonal antibody targeted drug.



Figure 4. E.Cotector

Transmembrane Protein of scFv

To display scFv on the surface of E.coli, we use a transmembrane protein. The transmembrane protein is composed of lipoprotein (Lpp) and outer membrane protein A (OmpA) .



Figure 5. Figure 6. Transmembrane protein: Lpp-OmpA is composed of lipoprotein (Lpp) and outer membrane protein A (OmpA) .

Lpp-OmpA was designed as a fusion protein consisting of the signal sequence and first 9 amino acids of Lpp, residue 46~159 of OmpA. The Lpp of the N-terminal of this fusion protein targets the protein on the membrane while the transmembrane domain of OmpA serves as an anchor. ScFv is on the externally exposed loops of C-terminal of OmpA, which can be anchored to the outer membrane. Between the OmpA and scFv, there is a cutting site of restriction enzyme called NcoI. With this cutting site, the linked scFv can be easily changed like a cassette. [1]







Figure 7. To change the scFv sequence easily, we designed the NcoI restriction site between Lpp-Omp A and scFv. When designing XbaI-SpeI restriction site between Lpp-OmpA and scFv, it cause mixed site. Therefore, NcoI restriction site rather than EX-SP restriction site was designed.

Color Signal

The color signals that we have selected are fluorescence proteins and chromoproteins. Cooperating with iGEM, all of resources were from the giant registry of iGEM which is accessible to every iGEMer. APOllO utilized the red flourescent protein BBa_E1010, the green fluorescent protein BBa_E0040, the blue fluorescent protein BBa_K592100 , and the blue chromoprotein BBa_K592009.

Jump to Results



Figure 8. Different Color Signal

Gold Binding Polypeptide

Another plasmid is gold binding polypeptide, abbreviated as GBP. APOllO may display GBP on the surface of E. coli for binding on gold surface.

GBP was designed with the three-repeated following 14 amino acid sequences: [MHGKTQATSGTIQS]. The binding sequence of GBP does not contain cysteine which can form a covalent thiol linkage with gold, the linkage to the gold surface in Self-Assembled Monolayers (SAMs) [2].

The mechanism of the connection between GBP and gold metal plane remains unknown. By using Molecular Dynamics (MD), it indicates that GBP, with an antiparallel β-sheet structure, can recognize gold surface via OH-binding. It is likely that the hydroxyl, together with amine, ligands on GBP recognize the atomic lattice of gold, aligning the molecule along the variants of a six-fold axis on the Au (111) surface [3].



Figure 9. GBP can recognize and bind on the gold surface.

Transmembrane Protein of GBP

To display the GBP to the outer membrane of E.Cotector, we use a transmembrane protein called Long-chain fatty acid short as FadL. We selected the first 384 amino acid sequence from the FadL for the transmembrane protein of GBP.



Transmembrane Protein FadL transports GBP out of the surface of E. coli

Application: Immobilize on Gold

Via concept of biosensor, APOllO’s customers may deem the E.Cotector to play the role of biological recognition part and the gold chip to act as the signal transducer part. Combining with multiple physicochemical nanoscale detectors in various fields, such as optical, electrochemistry, microbalance and etcetera, greater precision and accuracy will be achieved.

Jump to Results



Figure 10. Concept of Biosensor via E.Cotector